A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288672



Internal ID20497890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3326176..3326456hg38UCSC Ensembl
chrX:3244217..3244497hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757482
Supporting Variants
Samples
Known GenesMXRA5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288672
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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